Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9147 |
| ensemblid | ENSG00000165525.18 |
| hgncid | 10663 |
| symbol | NEMF |
| name | nuclear export mediator factor |
| refseq_nuc | NM_004713.6 |
| refseq_prot | NP_004704.3 |
| ensembl_nuc | ENST00000298310.10 |
| ensembl_prot | ENSP00000298310.5 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 49782083 |
| end | 49852788 |
| strand | - |
| ver | v1.2 |
| region | chr14:49782083-49852788 |
| region5000 | chr14:49777083-49857788 |
| regionname0 | NEMF_chr14_49782083_49852788 |
| regionname5000 | NEMF_chr14_49777083_49857788 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1076 | 191 | 58 | 56 | 52 | 8 | 16 | 28 | NEMF_chr14_49777083_49857788 | NEMF | MKSRF others(1071): Show |
chr14 | 49777083 | 49857788 |
| a0002 | 1/0 | 1076 | 28 | 23 | 0 | 4 | 0 | 0 | 3 | NEMF_chr14_49777083_49857788 | NEMF | MKSRF others(1071): Show |
chr14 | 49777083 | 49857788 |
| a0003 | 0/0 | 1076 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | MKSRF others(1071): Show |
chr14 | 49777083 | 49857788 |
| a0004 | 0/0 | 1076 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | MKSRF others(1071): Show |
chr14 | 49777083 | 49857788 |
| a0005 | 0/0 | 1076 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEMF_chr14_49777083_49857788 | NEMF | MKSRF others(1071): Show |
chr14 | 49777083 | 49857788 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3228 | 180 | 51 | 54 | 50 | 8 | 16 | NEMF_chr14_49777083_49857788 | NEMF | ATGAA others(3223): Show |
chr14 | 49777083 | 49857788 | ||
| a0001c0004 | 0/0 | 3228 | 6 | 6 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | ATGAA others(3223): Show |
chr14 | 49777083 | 49857788 | ||
| a0001c0005 | 0/0 | 3228 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | ATGAA others(3223): Show |
chr14 | 49777083 | 49857788 | ||
| a0001c0009 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | ATGAA others(3223): Show |
chr14 | 49777083 | 49857788 | ||
| a0001c0010 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | ATGAA others(3223): Show |
chr14 | 49777083 | 49857788 | ||
| a0001c0011 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | ATGAA others(3223): Show |
chr14 | 49777083 | 49857788 | ||
| a0001c0012 | 0/0 | 3228 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | ATGAA others(3223): Show |
chr14 | 49777083 | 49857788 | ||
| a0002c0002 | 1/0 | 3228 | 15 | 10 | 0 | 4 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | ATGAA others(3223): Show |
chr14 | 49777083 | 49857788 | ||
| a0002c0003 | 0/0 | 3228 | 13 | 13 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | ATGAA others(3223): Show |
chr14 | 49777083 | 49857788 | ||
| a0003c0008 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | ATGAA others(3223): Show |
chr14 | 49777083 | 49857788 | ||
| a0004c0006 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | ATGAA others(3223): Show |
chr14 | 49777083 | 49857788 | ||
| a0005c0007 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | ATGAA others(3223): Show |
chr14 | 49777083 | 49857788 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5818 | 118 | 32 | 29 | 39 | 4 | 14 | NEMF_chr14_49777083_49857788 | NEMF | AGAGG others(5813): Show |
chr14 | 49777083 | 49857788 |
| a0001c0001t0002 | 0/0 | 5819 | 33 | 9 | 13 | 10 | 1 | 0 | NEMF_chr14_49777083_49857788 | NEMF | AGAGG others(5814): Show |
chr14 | 49777083 | 49857788 |
| a0001c0001t0003 | 0/0 | 5818 | 25 | 8 | 12 | 1 | 3 | 1 | NEMF_chr14_49777083_49857788 | NEMF | AGAGG others(5813): Show |
chr14 | 49777083 | 49857788 |
| a0001c0001t0006 | 0/0 | 5819 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | AGAGG others(5814): Show |
chr14 | 49777083 | 49857788 |
| a0001c0001t0007 | 0/0 | 5818 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | AGAGG others(5813): Show |
chr14 | 49777083 | 49857788 |
| a0001c0001t0008 | 0/1 | 5815 | 1 | 0 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | AGAGG others(5810): Show |
chr14 | 49777083 | 49857788 |
| a0001c0001t0009 | 0/0 | 5818 | 1 | 0 | 0 | 0 | 0 | 1 | NEMF_chr14_49777083_49857788 | NEMF | AGAGG others(5813): Show |
chr14 | 49777083 | 49857788 |
| a0001c0004t0002 | 0/0 | 5819 | 6 | 6 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | AGAGG others(5814): Show |
chr14 | 49777083 | 49857788 |
| a0001c0005t0001 | 0/0 | 5818 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | AGAGG others(5813): Show |
chr14 | 49777083 | 49857788 |
| a0001c0009t0001 | 0/0 | 5818 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | AGAGG others(5813): Show |
chr14 | 49777083 | 49857788 |
| a0001c0010t0002 | 0/0 | 5819 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | AGAGG others(5814): Show |
chr14 | 49777083 | 49857788 |
| a0001c0011t0001 | 0/0 | 5818 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | AGAGG others(5813): Show |
chr14 | 49777083 | 49857788 |
| a0001c0012t0001 | 0/0 | 5818 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | AGAGG others(5813): Show |
chr14 | 49777083 | 49857788 |
| a0002c0002t0001 | 0/0 | 5818 | 10 | 10 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | AGAGG others(5813): Show |
chr14 | 49777083 | 49857788 |
| a0002c0002t0005 | 0/0 | 5818 | 4 | 0 | 0 | 4 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | AGAGG others(5813): Show |
chr14 | 49777083 | 49857788 |
| a0002c0002t0011 | 1/0 | 5819 | 1 | 0 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | AGAGG others(5814): Show |
chr14 | 49777083 | 49857788 |
| a0002c0003t0004 | 0/0 | 5824 | 12 | 12 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | AGAGG others(5819): Show |
chr14 | 49777083 | 49857788 |
| a0002c0003t0010 | 0/0 | 5819 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | AGAGG others(5814): Show |
chr14 | 49777083 | 49857788 |
| a0003c0008t0001 | 0/0 | 5818 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | AGAGG others(5813): Show |
chr14 | 49777083 | 49857788 |
| a0004c0006t0002 | 0/0 | 5819 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | AGAGG others(5814): Show |
chr14 | 49777083 | 49857788 |
| a0005c0007t0002 | 0/0 | 5819 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | AGAGG others(5814): Show |
chr14 | 49777083 | 49857788 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0008g0208 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0001t0009g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0004t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0004t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0004t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0004t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0004t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0004t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0005t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0009t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0010t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0011t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0001c0012t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0002t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0002t0005g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0002t0005g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0002t0005g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0002t0011g0214 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0003t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0003t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0003t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0003t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0003t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0003t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0003t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0003t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0003t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0003t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0003t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0003t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0002c0003t0010g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0003c0008t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0004c0006t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| a0005c0007t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | FIN | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | FIN | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0151 | EUR | FIN | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | FIN | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00544 | hp1 | a0001 | c0010 | t0002 | g0169 | EAS | CHS | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00597 | hp2 | a0002 | c0002 | t0005 | g0006 | EAS | CHS | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | CHS | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0187 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0177 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | CHS | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0193 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0189 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0179 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01081 | hp1 | a0001 | c0012 | t0001 | g0170 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0185 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0195 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0180 | AMR | CLM | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | CLM | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0178 | AMR | CLM | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | CLM | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01496 | hp2 | a0001 | c0005 | t0001 | g0140 | AMR | CLM | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | ACB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01891 | hp2 | a0002 | c0003 | t0004 | g0219 | AFR | ACB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PEL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | PEL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02040 | hp2 | a0003 | c0008 | t0001 | g0142 | EAS | KHV | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | ACB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0137 | AFR | ACB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0206 | AFR | ACB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0204 | AFR | ACB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0199 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02572 | hp2 | a0002 | c0003 | t0004 | g0215 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02602 | hp2 | a0001 | c0001 | t0009 | g0013 | SAS | PJL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0207 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02630 | hp2 | a0002 | c0003 | t0004 | g0221 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0201 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02809 | hp1 | a0002 | c0003 | t0004 | g0210 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02886 | hp2 | a0001 | c0004 | t0002 | g0037 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02895 | hp1 | a0002 | c0003 | t0004 | g0211 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02896 | hp2 | a0002 | c0003 | t0004 | g0216 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02922 | hp1 | a0001 | c0011 | t0001 | g0083 | AFR | ESN | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02922 | hp2 | a0002 | c0003 | t0004 | g0218 | AFR | ESN | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0205 | AFR | ESN | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0138 | AFR | ESN | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03041 | hp2 | a0001 | c0004 | t0002 | g0034 | AFR | GWD | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03098 | hp1 | a0002 | c0003 | t0010 | g0175 | AFR | MSL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03098 | hp2 | a0002 | c0003 | t0004 | g0209 | AFR | MSL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ESN | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03139 | hp1 | a0002 | c0003 | t0004 | g0217 | AFR | ESN | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03209 | hp1 | a0004 | c0006 | t0002 | g0025 | AFR | MSL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03209 | hp2 | a0002 | c0003 | t0004 | g0220 | AFR | MSL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | MSL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0191 | SAS | PJL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03453 | hp1 | a0002 | c0003 | t0004 | g0212 | AFR | MSL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0190 | AFR | ESN | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03516 | hp2 | a0001 | c0004 | t0002 | g0036 | AFR | ESN | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0203 | AFR | MSL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | STU | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | STU | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | STU | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0200 | AFR | YRI | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0183 | AFR | YRI | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19007 | hp2 | a0001 | c0009 | t0001 | g0092 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19011 | hp2 | a0002 | c0002 | t0005 | g0004 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19012 | hp1 | a0005 | c0007 | t0002 | g0163 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19043 | hp2 | a0002 | c0003 | t0004 | g0213 | AFR | LWK | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19076 | hp1 | a0002 | c0002 | t0005 | g0007 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19081 | hp1 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA19240 | hp2 | a0001 | c0004 | t0002 | g0016 | AFR | YRI | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ASW | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0196 | AFR | ASW | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | TSI | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0182 | EUR | TSI | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0184 | EUR | TSI | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | GIH | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | GIH | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | ACB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0186 | AFR | ACB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG02559 | hp2 | a0001 | c0004 | t0002 | g0032 | AFR | ACB | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03471 | hp1 | a0001 | c0004 | t0002 | g0035 | AFR | MSL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | USA | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | USA | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0202 | AFR | USA | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | USA | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0008 | g0208 | REF | REF | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0011 | g0214 | REF | REF | NEMF_chr14_49777083_49857788 | NEMF | chr14 | 49777083 | 49857788 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:49795812 | C | G | 1 | a0003 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.2598G>C | p.Gln866His | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/33 | 2633/5819 | 2598/3231 | 866/1076 | chr14 | 49795812 | |||
| chr14:49795922 | G | T | 1 | a0005 | 1 | NA19012.hp1 | missense_variant | MODERATE | c.2488C>A | p.Pro830Thr | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/33 | 2523/5819 | 2488/3231 | 830/1076 | chr14 | 49795922 | |||
| chr14:49800475 | C | T | 1 | a0004 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.2317G>A | p.Glu773Lys | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 23/33 | 2352/5819 | 2317/3231 | 773/1076 | chr14 | 49800475 | |||
| chr14:49832244 | T | A | 4 | a0001 a0003 a0004 others(1): Show |
193 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
missense_variant | MODERATE | c.769A>T | p.Ser257Cys | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 9/33 | 804/5819 | 769/3231 | 257/1076 | chr14 | 49832244 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:49784651 | G | A | 1 | a0002c0003 | 13 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(10): Show |
synonymous_variant | LOW | c.3216C>T | p.Asn1072Asn | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 33/33 | 3251/5819 | 3216/3231 | 1072/1076 | chr14 | 49784651 | |||
| chr14:49784952 | T | C | 1 | a0001c0004 | 6 | HG02559.hp2 HG02886.hp2 HG03041.hp2 others(3): Show |
synonymous_variant | LOW | c.3126A>G | p.Arg1042Arg | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 32/33 | 3161/5819 | 3126/3231 | 1042/1076 | chr14 | 49784952 | |||
| chr14:49795809 | T | A | 1 | a0001c0009 | 1 | NA19007.hp2 | synonymous_variant | LOW | c.2601A>T | p.Pro867Pro | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/33 | 2636/5819 | 2601/3231 | 867/1076 | chr14 | 49795809 | |||
| chr14:49795911 | T | A | 1 | a0001c0010 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.2499A>T | p.Ser833Ser | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/33 | 2534/5819 | 2499/3231 | 833/1076 | chr14 | 49795911 | |||
| chr14:49802717 | A | G | 1 | a0001c0005 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.1926T>C | p.Asn642Asn | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 21/33 | 1961/5819 | 1926/3231 | 642/1076 | chr14 | 49802717 | |||
| chr14:49832087 | T | G | 1 | a0001c0011 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.846A>C | p.Ser282Ser | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 10/33 | 881/5819 | 846/3231 | 282/1076 | chr14 | 49832087 | |||
| chr14:49851569 | G | C | 1 | a0001c0012 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.225C>G | p.Ala75Ala | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/33 | 260/5819 | 225/3231 | 75/1076 | chr14 | 49851569 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:49782669 | G | A | 1 | a0002c0003t0010 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1967C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 33/33 | 1967 | chr14 | 49782669 | ||||||
| chr14:49782782 | C | CCAAA | 1 | a0002c0003t0004 | 12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1850_*1853dupTTTG | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 33/33 | 1853 | chr14 | 49782782 | ||||||
| chr14:49783336 | G | A | 1 | a0001c0001t0009 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1300C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 33/33 | 1300 | chr14 | 49783336 | ||||||
| chr14:49783340 | C | T | 1 | a0002c0002t0005 | 4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1296G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 33/33 | 1296 | chr14 | 49783340 | ||||||
| chr14:49783369 | GT | G | 11 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(8): Show |
164 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*1266delA | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 33/33 | 1266 | chr14 | 49783369 | ||||||
| chr14:49783371 | T | G | 2 | a0001c0001t0003 a0001c0001t0007 |
26 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1265A>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 33/33 | 1265 | chr14 | 49783371 | ||||||
| chr14:49783501 | T | TA | 1 | a0002c0003t0004 | 12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1134dupT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 33/33 | 1134 | chr14 | 49783501 | ||||||
| chr14:49783694 | A | G | 1 | a0001c0001t0007 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*942T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 33/33 | 942 | chr14 | 49783694 | ||||||
| chr14:49784075 | C | T | 17 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(14): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*561G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 33/33 | 561 | chr14 | 49784075 | ||||||
| chr14:49784571 | C | G | 1 | a0001c0001t0006 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*65G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 33/33 | 65 | chr14 | 49784571 | ||||||
| chr14:49852781 | G | T | 18 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(15): Show |
208 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
5_prime_UTR_variant | MODIFIER | c.-28C>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 1/33 | 28 | chr14 | 49852781 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:49784798 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3154-85T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 32/32 | chr14 | 49784798 | |||||||
| chr14:49785170 | C | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.3030-35G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 30/32 | chr14 | 49785170 | |||||||
| chr14:49785456 | A | ACTT | 4 | a0001c0001t0001g0017 a0001c0001t0001g0060 a0001c0001t0001g0127 others(1): Show |
4 | HG00544.hp1 HG00544.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.2929-139_2929-137d others(5): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 29/32 | chr14 | 49785456 | |||||||
| chr14:49785575 | T | TAC | 4 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0002g0014 others(1): Show |
4 | HG02615.hp1 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.2929-257_2929-256d others(4): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 29/32 | chr14 | 49785575 | |||||||
| chr14:49785778 | G | A | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(202): Show |
206 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.2929-458C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 29/32 | chr14 | 49785778 | |||||||
| chr14:49785889 | C | CA | 29 | a0001c0001t0001g0046 a0001c0001t0001g0128 a0001c0001t0001g0129 others(26): Show |
29 | HG00597.hp2 HG01123.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.2929-570dupT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 29/32 | chr14 | 49785889 | |||||||
| chr14:49785889 | C | CAA | 184 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(181): Show |
185 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.2929-571_2929-570d others(4): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 29/32 | chr14 | 49785889 | |||||||
| chr14:49785909 | A | G | 1 | a0001c0001t0003g0193 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2929-589T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 29/32 | chr14 | 49785909 | |||||||
| chr14:49785945 | T | C | 3 | a0001c0001t0001g0136 a0001c0001t0001g0146 a0001c0012t0001g0170 |
3 | HG00741.hp1 HG01081.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.2929-625A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 29/32 | chr14 | 49785945 | |||||||
| chr14:49786041 | G | A | 8 | a0001c0001t0001g0101 a0002c0003t0004g0215 a0002c0003t0004g0216 others(5): Show |
8 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2928+677C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 29/32 | chr14 | 49786041 | |||||||
| chr14:49786143 | G | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2928+575C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 29/32 | chr14 | 49786143 | |||||||
| chr14:49786308 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2928+410T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 29/32 | chr14 | 49786308 | |||||||
| chr14:49787005 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(191): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.2896-255C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49787005 | |||||||
| chr14:49787372 | T | C | 54 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(51): Show |
54 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2896-622A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49787372 | |||||||
| chr14:49787437 | G | A | 1 | a0001c0001t0003g0192 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2896-687C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49787437 | |||||||
| chr14:49787553 | C | T | 1 | a0002c0003t0010g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2896-803G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49787553 | |||||||
| chr14:49787586 | G | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2896-836C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49787586 | |||||||
| chr14:49787802 | C | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2896-1052G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49787802 | |||||||
| chr14:49787979 | C | T | 1 | a0002c0003t0004g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2895+1167G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49787979 | |||||||
| chr14:49788009 | T | A | 1 | a0002c0002t0001g0200 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2895+1137A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788009 | |||||||
| chr14:49788147 | T | C | 168 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(165): Show |
168 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.2895+999A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788147 | |||||||
| chr14:49788216 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2895+930A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788216 | |||||||
| chr14:49788250 | G | A | 7 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(4): Show |
7 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2895+896C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788250 | |||||||
| chr14:49788266 | A | G | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(196): Show |
200 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.2895+880T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788266 | |||||||
| chr14:49788276 | C | CA | 13 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(10): Show |
13 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.2895+869dupT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788276 | |||||||
| chr14:49788276 | C | CAAA | 6 | a0002c0002t0001g0201 a0002c0002t0001g0202 a0002c0002t0001g0203 others(3): Show |
6 | HG02451.hp1 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2895+867_2895+869d others(5): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788276 | |||||||
| chr14:49788276 | C | CAAAA | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(156): Show |
160 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.2895+866_2895+869d others(6): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788276 | |||||||
| chr14:49788276 | C | CAAAAA | 34 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0051 others(31): Show |
34 | HG00609.hp2 HG00621.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.2895+865_2895+869d others(7): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788276 | |||||||
| chr14:49788276 | CAAAAAAA others(3): Show |
C | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.2895+860_2895+869d others(12): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788276 | |||||||
| chr14:49788296 | A | T | 1 | a0001c0001t0001g0043 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2895+850T>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788296 | |||||||
| chr14:49788548 | TTC | T | 34 | a0001c0001t0002g0022 a0001c0001t0002g0084 a0001c0001t0003g0001 others(31): Show |
35 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.2895+596_2895+597d others(4): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788548 | |||||||
| chr14:49788557 | TC | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(109): Show |
112 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.2895+588delG | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788557 | |||||||
| chr14:49788558 | CT | C | 71 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0018 others(68): Show |
71 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.2895+587delA | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788558 | |||||||
| chr14:49788596 | C | T | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.2895+550G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788596 | |||||||
| chr14:49788597 | G | A | 1 | a0002c0003t0010g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2895+549C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788597 | |||||||
| chr14:49788614 | G | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2895+532C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788614 | |||||||
| chr14:49788715 | C | T | 3 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0099 |
3 | HG02056.hp1 HG02080.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2895+431G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788715 | |||||||
| chr14:49788760 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2895+386G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788760 | |||||||
| chr14:49788794 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2895+352A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788794 | |||||||
| chr14:49788846 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2895+300G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788846 | |||||||
| chr14:49788874 | T | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2895+272A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788874 | |||||||
| chr14:49788882 | C | G | 1 | a0002c0003t0004g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2895+264G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788882 | |||||||
| chr14:49788907 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2895+239T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788907 | |||||||
| chr14:49788926 | G | A | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0002g0112 |
3 | HG02280.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2895+220C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49788926 | |||||||
| chr14:49789115 | T | TAAGAAGC others(318): Show |
1 | a0001c0001t0001g0102 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2895+30_2895+31ins others(325): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49789115 | |||||||
| chr14:49789122 | C | G | 1 | a0002c0003t0010g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2895+24G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 28/32 | chr14 | 49789122 | |||||||
| chr14:49790078 | A | G | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2620-505T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49790078 | |||||||
| chr14:49790086 | GA | G | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG02622.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2620-514delT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49790086 | |||||||
| chr14:49790143 | G | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2620-570C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49790143 | |||||||
| chr14:49790668 | G | C | 3 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0007 |
3 | NA19011.hp2 NA19076.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2620-1095C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49790668 | |||||||
| chr14:49790721 | G | A | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.2620-1148C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49790721 | |||||||
| chr14:49791060 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2620-1487C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49791060 | |||||||
| chr14:49791139 | T | G | 1 | a0001c0011t0001g0083 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2620-1566A>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49791139 | |||||||
| chr14:49791203 | C | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2620-1630G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49791203 | |||||||
| chr14:49791227 | C | A | 1 | a0002c0003t0004g0210 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2620-1654G>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49791227 | |||||||
| chr14:49791505 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2620-1932C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49791505 | |||||||
| chr14:49791727 | A | C | 1 | a0001c0001t0001g0088 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2620-2154T>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49791727 | |||||||
| chr14:49791735 | TAAAAAA | T | 9 | a0001c0001t0001g0125 a0002c0002t0001g0200 a0002c0002t0001g0201 others(6): Show |
9 | HG02055.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2620-2168_2620-216 others(10): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49791735 | |||||||
| chr14:49791735 | TAAAAAAA | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(187): Show |
191 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.2620-2169_2620-216 others(11): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49791735 | |||||||
| chr14:49791735 | TAAAAAAA others(1): Show |
T | 6 | a0001c0001t0001g0055 a0001c0001t0001g0086 a0001c0001t0002g0166 others(3): Show |
6 | HG00323.hp2 HG00597.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.2620-2170_2620-216 others(12): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49791735 | |||||||
| chr14:49791743 | A | T | 1 | a0001c0001t0003g0199 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2620-2170T>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49791743 | |||||||
| chr14:49792800 | G | C | 4 | a0001c0001t0001g0081 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG01433.hp2 HG02055.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2619+2991C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49792800 | |||||||
| chr14:49792819 | A | G | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2619+2972T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49792819 | |||||||
| chr14:49792848 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2619+2943C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49792848 | |||||||
| chr14:49792914 | G | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2619+2877C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49792914 | |||||||
| chr14:49792946 | A | G | 169 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(166): Show |
169 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.2619+2845T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49792946 | |||||||
| chr14:49792964 | G | A | 7 | a0001c0001t0003g0177 a0001c0001t0003g0178 a0001c0001t0003g0184 others(4): Show |
7 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.2619+2827C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49792964 | |||||||
| chr14:49793086 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2619+2705T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49793086 | |||||||
| chr14:49793100 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0094 |
2 | HG01346.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.2619+2691C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49793100 | |||||||
| chr14:49793453 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2619+2338G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49793453 | |||||||
| chr14:49793714 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2619+2077G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49793714 | |||||||
| chr14:49793744 | A | T | 1 | a0001c0001t0001g0161 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2619+2047T>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49793744 | |||||||
| chr14:49793861 | T | C | 25 | a0001c0001t0003g0001 a0001c0001t0003g0176 a0001c0001t0003g0177 others(22): Show |
26 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.2619+1930A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49793861 | |||||||
| chr14:49793875 | T | C | 1 | a0001c0001t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2619+1916A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49793875 | |||||||
| chr14:49793876 | C | G | 70 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0018 others(67): Show |
70 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.2619+1915G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49793876 | |||||||
| chr14:49793906 | CT | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2619+1884delA | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49793906 | |||||||
| chr14:49793988 | T | C | 12 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(9): Show |
12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2619+1803A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49793988 | |||||||
| chr14:49794064 | G | A | 8 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2619+1727C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49794064 | |||||||
| chr14:49794325 | G | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2619+1466C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49794325 | |||||||
| chr14:49794619 | T | TA | 7 | a0001c0001t0001g0049 a0001c0001t0001g0053 a0001c0001t0001g0071 others(4): Show |
7 | HG01175.hp2 HG02083.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.2619+1171dupT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49794619 | |||||||
| chr14:49794619 | TA | T | 16 | a0001c0001t0001g0056 a0001c0001t0002g0151 a0001c0001t0002g0153 others(13): Show |
16 | HG00323.hp1 HG01257.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2619+1171delT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49794619 | |||||||
| chr14:49794718 | C | CT | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(169): Show |
172 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.2619+1072dupA | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49794718 | |||||||
| chr14:49794718 | C | CTT | 34 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0109 others(31): Show |
35 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.2619+1071_2619+107 others(6): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49794718 | |||||||
| chr14:49794903 | G | C | 2 | a0002c0003t0004g0215 a0002c0003t0004g0219 |
2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2619+888C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49794903 | |||||||
| chr14:49794967 | C | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2619+824G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49794967 | |||||||
| chr14:49795061 | G | A | 12 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(9): Show |
12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2619+730C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49795061 | |||||||
| chr14:49795516 | CT | C | 8 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2619+274delA | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49795516 | |||||||
| chr14:49795771 | T | C | 2 | a0001c0001t0003g0198 a0001c0001t0003g0199 |
2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2619+20A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 26/32 | chr14 | 49795771 | |||||||
| chr14:49796107 | T | C | 1 | a0001c0001t0002g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2466-163A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49796107 | |||||||
| chr14:49796479 | T | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0060 a0001c0001t0001g0127 |
3 | HG00544.hp2 HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2466-535A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49796479 | |||||||
| chr14:49796487 | A | T | 1 | a0001c0001t0001g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2466-543T>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49796487 | |||||||
| chr14:49796550 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0130 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2466-606G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49796550 | |||||||
| chr14:49796576 | T | C | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(164): Show |
167 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.2466-632A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49796576 | |||||||
| chr14:49797091 | A | C | 1 | a0001c0001t0001g0049 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2466-1147T>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49797091 | |||||||
| chr14:49797150 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2466-1206G>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49797150 | |||||||
| chr14:49797233 | T | G | 25 | a0001c0001t0003g0001 a0001c0001t0003g0176 a0001c0001t0003g0177 others(22): Show |
26 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.2466-1289A>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49797233 | |||||||
| chr14:49797279 | T | C | 12 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(9): Show |
12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2466-1335A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49797279 | |||||||
| chr14:49797332 | T | TA | 6 | a0001c0001t0001g0054 a0001c0001t0001g0066 a0001c0001t0001g0067 others(3): Show |
6 | HG02809.hp2 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2466-1389dupT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49797332 | |||||||
| chr14:49797382 | A | G | 1 | a0002c0003t0010g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2466-1438T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49797382 | |||||||
| chr14:49797447 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2466-1503G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49797447 | |||||||
| chr14:49797475 | C | A | 1 | a0001c0001t0001g0048 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2466-1531G>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49797475 | |||||||
| chr14:49797601 | G | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2466-1657C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49797601 | |||||||
| chr14:49798325 | T | C | 3 | a0001c0001t0001g0105 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | HG01069.hp2 HG01255.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.2465+1150A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49798325 | |||||||
| chr14:49798355 | C | T | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.2465+1120G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49798355 | |||||||
| chr14:49798634 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0002g0089 |
2 | NA18994.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.2465+841G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49798634 | |||||||
| chr14:49798689 | C | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2465+786G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49798689 | |||||||
| chr14:49798701 | A | G | 12 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(9): Show |
12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2465+774T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49798701 | |||||||
| chr14:49798765 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2465+710C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49798765 | |||||||
| chr14:49799091 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2465+384G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49799091 | |||||||
| chr14:49799165 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2465+310C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49799165 | |||||||
| chr14:49799184 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2465+291C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49799184 | |||||||
| chr14:49799207 | C | CA | 23 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0045 others(20): Show |
23 | HG00673.hp1 HG00673.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.2465+267dupT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49799207 | |||||||
| chr14:49799207 | C | CAA | 11 | a0001c0001t0001g0041 a0001c0001t0001g0097 a0001c0001t0001g0106 others(8): Show |
11 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.2465+266_2465+267d others(4): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49799207 | |||||||
| chr14:49799207 | C | CAAA | 28 | a0001c0001t0001g0098 a0001c0001t0001g0120 a0001c0001t0001g0131 others(25): Show |
29 | HG00280.hp1 HG00738.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.2465+265_2465+267d others(5): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49799207 | |||||||
| chr14:49799207 | C | CAAAA | 50 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(47): Show |
50 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.2465+264_2465+267d others(6): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49799207 | |||||||
| chr14:49799207 | C | CAAAAA | 28 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0033 others(25): Show |
28 | HG00544.hp2 HG00741.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.2465+263_2465+267d others(7): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49799207 | |||||||
| chr14:49799207 | C | CAAAAAA | 15 | a0001c0001t0001g0101 a0001c0001t0001g0155 a0001c0001t0002g0023 others(12): Show |
15 | HG00323.hp1 HG00544.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2465+262_2465+267d others(8): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49799207 | |||||||
| chr14:49799207 | C | CAAAAAAA | 10 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0020 others(7): Show |
10 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.2465+261_2465+267d others(9): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49799207 | |||||||
| chr14:49799207 | C | CAAAAAAA others(3): Show |
1 | a0002c0002t0005g0007 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2465+258_2465+267d others(12): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49799207 | |||||||
| chr14:49799373 | GA | G | 169 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(166): Show |
169 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.2465+101delT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49799373 | |||||||
| chr14:49799377 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(191): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.2465+98C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 25/32 | chr14 | 49799377 | |||||||
| chr14:49799918 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2373-240G>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 23/32 | chr14 | 49799918 | |||||||
| chr14:49800961 | T | C | 1 | a0001c0001t0006g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2096-265A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 22/32 | chr14 | 49800961 | |||||||
| chr14:49801077 | G | C | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.2096-381C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 22/32 | chr14 | 49801077 | |||||||
| chr14:49801134 | T | C | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(164): Show |
167 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.2096-438A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 22/32 | chr14 | 49801134 | |||||||
| chr14:49801317 | G | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2096-621C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 22/32 | chr14 | 49801317 | |||||||
| chr14:49801492 | GA | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(179): Show |
182 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.2096-797delT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 22/32 | chr14 | 49801492 | |||||||
| chr14:49801492 | GAA | G | 6 | a0001c0001t0001g0097 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG00609.hp2 HG01952.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.2096-798_2096-797d others(4): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 22/32 | chr14 | 49801492 | |||||||
| chr14:49801493 | A | G | 26 | a0001c0001t0003g0001 a0001c0001t0003g0176 a0001c0001t0003g0179 others(23): Show |
27 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.2096-797T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 22/32 | chr14 | 49801493 | |||||||
| chr14:49801494 | A | G | 7 | a0001c0001t0003g0177 a0001c0001t0003g0178 a0001c0001t0003g0184 others(4): Show |
7 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.2096-798T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 22/32 | chr14 | 49801494 | |||||||
| chr14:49801820 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2095+633T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 22/32 | chr14 | 49801820 | |||||||
| chr14:49801859 | C | A | 1 | a0001c0001t0001g0075 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2095+594G>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 22/32 | chr14 | 49801859 | |||||||
| chr14:49801954 | CT | C | 21 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0064 others(18): Show |
21 | HG00639.hp2 HG01074.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.2095+498delA | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 22/32 | chr14 | 49801954 | |||||||
| chr14:49801978 | G | T | 1 | a0002c0003t0004g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2095+475C>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 22/32 | chr14 | 49801978 | |||||||
| chr14:49802072 | C | G | 1 | a0001c0001t0002g0019 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2095+381G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 22/32 | chr14 | 49802072 | |||||||
| chr14:49802299 | AAAAAAAA others(32): Show |
A | 1 | a0001c0001t0001g0065 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2095+115_2095+153d others(41): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 22/32 | chr14 | 49802299 | |||||||
| chr14:49802337 | T | C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2095+116A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 22/32 | chr14 | 49802337 | |||||||
| chr14:49802600 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1975-27G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 21/32 | chr14 | 49802600 | |||||||
| chr14:49803126 | T | C | 8 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1915+111A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 20/32 | chr14 | 49803126 | |||||||
| chr14:49803363 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1858-69C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 19/32 | chr14 | 49803363 | |||||||
| chr14:49803486 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1858-192T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 19/32 | chr14 | 49803486 | |||||||
| chr14:49803628 | T | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1858-334A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 19/32 | chr14 | 49803628 | |||||||
| chr14:49803710 | G | C | 8 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1858-416C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 19/32 | chr14 | 49803710 | |||||||
| chr14:49804007 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1858-713G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 19/32 | chr14 | 49804007 | |||||||
| chr14:49804165 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1858-871G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 19/32 | chr14 | 49804165 | |||||||
| chr14:49804354 | A | G | 1 | a0001c0001t0002g0112 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1858-1060T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 19/32 | chr14 | 49804354 | |||||||
| chr14:49804575 | A | AGAATTGC others(27): Show |
1 | a0001c0001t0001g0065 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1858-1315_1858-128 others(38): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 19/32 | chr14 | 49804575 | |||||||
| chr14:49804667 | T | TA | 193 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(190): Show |
194 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.1857+1353dupT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 19/32 | chr14 | 49804667 | |||||||
| chr14:49804945 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1857+1076C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 19/32 | chr14 | 49804945 | |||||||
| chr14:49805046 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0099 |
2 | HG02056.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1857+975G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 19/32 | chr14 | 49805046 | |||||||
| chr14:49805207 | T | C | 12 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(9): Show |
12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1857+814A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 19/32 | chr14 | 49805207 | |||||||
| chr14:49805461 | G | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(195): Show |
199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1857+560C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 19/32 | chr14 | 49805461 | |||||||
| chr14:49805587 | A | C | 8 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1857+434T>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 19/32 | chr14 | 49805587 | |||||||
| chr14:49805620 | T | G | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1857+401A>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 19/32 | chr14 | 49805620 | |||||||
| chr14:49805626 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(191): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1857+395T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 19/32 | chr14 | 49805626 | |||||||
| chr14:49805873 | T | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0159 |
2 | HG00621.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1857+148A>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 19/32 | chr14 | 49805873 | |||||||
| chr14:49806230 | G | GTATATAT others(5): Show |
1 | a0002c0003t0004g0210 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1745-98_1745-97ins others(12): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806230 | |||||||
| chr14:49806230 | G | GTATATAT others(7): Show |
1 | a0002c0003t0004g0212 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1745-98_1745-97ins others(14): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806230 | |||||||
| chr14:49806230 | G | GTATATAT others(15): Show |
1 | a0002c0003t0004g0217 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1745-98_1745-97ins others(22): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806230 | |||||||
| chr14:49806230 | G | GTATATAT others(17): Show |
1 | a0002c0003t0004g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1745-98_1745-97ins others(24): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806230 | |||||||
| chr14:49806232 | G | A | 18 | a0001c0001t0001g0085 a0002c0002t0001g0200 a0002c0002t0001g0201 others(15): Show |
18 | HG00597.hp2 HG01928.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1745-99C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806232 | |||||||
| chr14:49806232 | G | GTATA | 4 | a0001c0001t0001g0043 a0001c0001t0001g0136 a0001c0001t0002g0014 others(1): Show |
4 | HG01123.hp1 HG02258.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1745-103_1745-100d others(6): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806232 | |||||||
| chr14:49806232 | G | GTATATAT others(1): Show |
7 | a0001c0001t0001g0129 a0001c0001t0003g0001 a0001c0001t0003g0180 others(4): Show |
8 | HG00280.hp1 HG00738.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1745-107_1745-100d others(10): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806232 | |||||||
| chr14:49806232 | G | GTATATAT others(3): Show |
5 | a0001c0001t0001g0033 a0001c0001t0001g0126 a0001c0001t0001g0127 others(2): Show |
5 | HG01168.hp2 HG04115.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1745-109_1745-100d others(12): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806232 | |||||||
| chr14:49806232 | G | GTATATAT others(7): Show |
7 | a0001c0001t0001g0047 a0001c0001t0001g0067 a0001c0001t0001g0068 others(4): Show |
7 | HG01167.hp1 HG01934.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1745-113_1745-100d others(16): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806232 | |||||||
| chr14:49806232 | G | GTATATAT others(9): Show |
5 | a0001c0001t0001g0054 a0001c0001t0001g0079 a0001c0001t0001g0111 others(2): Show |
5 | HG01258.hp2 HG02723.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1745-115_1745-100d others(18): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806232 | |||||||
| chr14:49806232 | G | GTATATAT others(11): Show |
2 | a0001c0001t0001g0070 a0001c0001t0001g0143 |
2 | HG00639.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1745-117_1745-100d others(20): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806232 | |||||||
| chr14:49806232 | G | GTATATAT others(13): Show |
12 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0057 others(9): Show |
12 | HG00609.hp1 HG01361.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1745-119_1745-100d others(22): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806232 | |||||||
| chr14:49806232 | G | GTATATAT others(15): Show |
5 | a0001c0001t0001g0044 a0001c0001t0001g0091 a0001c0001t0002g0023 others(2): Show |
5 | HG00558.hp2 HG01361.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1745-121_1745-100d others(24): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806232 | |||||||
| chr14:49806232 | G | GTATATAT others(17): Show |
4 | a0001c0001t0001g0077 a0001c0001t0001g0088 a0001c0001t0002g0020 others(1): Show |
4 | HG01175.hp1 HG02976.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1745-123_1745-100d others(26): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806232 | |||||||
| chr14:49806232 | G | GTATATAT others(19): Show |
3 | a0001c0001t0001g0122 a0001c0001t0002g0022 a0001c0001t0002g0084 |
3 | HG01074.hp1 HG01074.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1745-100_1745-99in others(27): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806232 | |||||||
| chr14:49806232 | G | GTATATAT others(21): Show |
1 | a0001c0001t0002g0151 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1745-100_1745-99in others(29): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806232 | |||||||
| chr14:49806232 | G | GTATATAT others(27): Show |
1 | a0002c0003t0004g0219 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1745-100_1745-99in others(35): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806232 | |||||||
| chr14:49806232 | G | GTGTATAT others(11): Show |
2 | a0001c0001t0001g0075 a0001c0001t0001g0174 |
2 | HG01258.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1745-100_1745-99in others(19): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806232 | |||||||
| chr14:49806232 | G | GTGTATAT others(13): Show |
1 | a0001c0001t0001g0093 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1745-100_1745-99in others(21): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806232 | |||||||
| chr14:49806232 | G | GTGTATAT others(15): Show |
1 | a0001c0001t0001g0050 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1745-100_1745-99in others(23): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806232 | |||||||
| chr14:49806232 | G | GTGTATAT others(21): Show |
1 | a0002c0003t0004g0216 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1745-100_1745-99in others(29): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806232 | |||||||
| chr14:49806232 | G | GTGTATAT others(33): Show |
1 | a0002c0003t0004g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1745-100_1745-99in others(41): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806232 | |||||||
| chr14:49806232 | G | GTGTGTAT others(21): Show |
1 | a0002c0003t0004g0221 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1745-100_1745-99in others(29): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806232 | |||||||
| chr14:49806232 | G | GTGTGTAT others(23): Show |
1 | a0002c0003t0004g0220 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1745-100_1745-99in others(31): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806232 | |||||||
| chr14:49806234 | A | G | 12 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0048 others(9): Show |
12 | HG01175.hp2 HG02257.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1745-101T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806234 | |||||||
| chr14:49806236 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1745-103T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806236 | |||||||
| chr14:49806246 | ATATATAT others(9): Show |
A | 1 | a0001c0004t0002g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1745-129_1745-114d others(18): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806246 | |||||||
| chr14:49806250 | ATATATAT others(6): Show |
A | 3 | a0001c0001t0001g0065 a0001c0001t0001g0120 a0001c0001t0001g0146 |
3 | HG00741.hp1 NA18980.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1745-130_1745-118d others(15): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806250 | |||||||
| chr14:49806250 | ATATATAT others(7): Show |
A | 1 | a0001c0012t0001g0170 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1745-131_1745-118d others(16): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806250 | |||||||
| chr14:49806250 | ATATATAT others(8): Show |
A | 1 | a0001c0001t0002g0021 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1745-132_1745-118d others(17): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806250 | |||||||
| chr14:49806252 | ATATATTT others(3): Show |
A | 2 | a0001c0001t0001g0017 a0001c0010t0002g0169 |
2 | HG00544.hp1 HG00544.hp2 |
intron_variant | MODIFIER | c.1745-129_1745-120d others(12): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806252 | |||||||
| chr14:49806254 | A | ATT | 5 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(2): Show |
5 | HG02257.hp1 HG02622.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1745-122_1745-121i others(4): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806254 | |||||||
| chr14:49806254 | A | T | 1 | a0002c0002t0001g0203 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1745-121T>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806254 | |||||||
| chr14:49806256 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0164 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1745-124_1745-123i others(25): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806256 | |||||||
| chr14:49806256 | A | T | 9 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(6): Show |
9 | HG00597.hp2 HG02257.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1745-123T>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806256 | |||||||
| chr14:49806257 | T | TA | 4 | a0001c0001t0001g0048 a0001c0001t0001g0063 a0001c0001t0001g0145 others(1): Show |
4 | HG01123.hp2 HG02451.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1745-125_1745-124i others(3): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806257 | |||||||
| chr14:49806257 | T | TATA | 3 | a0001c0001t0001g0042 a0001c0001t0001g0074 a0001c0001t0001g0094 |
3 | HG01346.hp2 HG01943.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1745-125_1745-124i others(5): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806257 | |||||||
| chr14:49806257 | T | TATATA | 9 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0001c0001t0001g0087 others(6): Show |
9 | HG01891.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1745-125_1745-124i others(7): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806257 | |||||||
| chr14:49806257 | T | TATATATA | 13 | a0001c0001t0001g0097 a0001c0001t0001g0125 a0001c0001t0001g0128 others(10): Show |
13 | HG00642.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1745-125_1745-124i others(9): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806257 | |||||||
| chr14:49806257 | T | TATATATA others(2): Show |
4 | a0001c0001t0001g0056 a0001c0001t0001g0101 a0001c0001t0001g0135 others(1): Show |
4 | HG01069.hp1 HG02735.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1745-125_1745-124i others(11): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806257 | |||||||
| chr14:49806257 | T | TATATATA others(4): Show |
8 | a0001c0001t0001g0018 a0001c0001t0001g0058 a0001c0001t0001g0161 others(5): Show |
8 | HG02109.hp1 HG02602.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1745-125_1745-124i others(13): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806257 | |||||||
| chr14:49806257 | T | TATATATA others(6): Show |
13 | a0001c0001t0001g0046 a0001c0001t0001g0061 a0001c0001t0001g0066 others(10): Show |
13 | HG01169.hp2 HG01934.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.1745-125_1745-124i others(15): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806257 | |||||||
| chr14:49806257 | T | TATATATA others(8): Show |
8 | a0001c0001t0001g0060 a0001c0001t0001g0130 a0001c0001t0001g0160 others(5): Show |
8 | HG00609.hp2 HG01169.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1745-125_1745-124i others(17): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806257 | |||||||
| chr14:49806257 | T | TATATATA others(10): Show |
7 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0100 others(4): Show |
7 | HG00621.hp2 HG01255.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1745-125_1745-124i others(19): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806257 | |||||||
| chr14:49806257 | T | TATATATA others(14): Show |
1 | a0001c0001t0001g0141 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1745-125_1745-124i others(23): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806257 | |||||||
| chr14:49806257 | T | TATATATA others(12): Show |
8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(5): Show |
8 | HG00673.hp2 HG01069.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1745-125_1745-124i others(21): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806257 | |||||||
| chr14:49806257 | T | TATATATA others(14): Show |
7 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0073 others(4): Show |
7 | HG00323.hp2 HG00597.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1745-125_1745-124i others(23): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806257 | |||||||
| chr14:49806257 | T | TATATATA others(16): Show |
10 | a0001c0001t0001g0040 a0001c0001t0001g0049 a0001c0001t0001g0064 others(7): Show |
10 | HG01952.hp2 HG02040.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.1745-125_1745-124i others(25): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806257 | |||||||
| chr14:49806257 | T | TATATATA others(18): Show |
7 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0072 others(4): Show |
7 | HG00621.hp1 HG01433.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.1745-125_1745-124i others(27): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806257 | |||||||
| chr14:49806257 | T | TATATATA others(20): Show |
1 | a0001c0001t0001g0059 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1745-125_1745-124i others(29): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806257 | |||||||
| chr14:49806257 | T | TATATATA others(22): Show |
2 | a0001c0001t0001g0158 a0002c0003t0004g0215 |
2 | HG01175.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1745-125_1745-124i others(31): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806257 | |||||||
| chr14:49806257 | T | TATATATA others(24): Show |
2 | a0001c0001t0001g0085 a0001c0001t0002g0089 |
2 | HG01928.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1745-125_1745-124i others(33): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806257 | |||||||
| chr14:49806257 | T | TATATATA others(34): Show |
1 | a0001c0001t0001g0038 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1745-125_1745-124i others(43): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806257 | |||||||
| chr14:49806258 | T | A | 60 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0041 others(57): Show |
60 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1745-125A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806258 | |||||||
| chr14:49806259 | T | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(97): Show |
100 | HG00323.hp2 HG00558.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.1745-126A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806259 | |||||||
| chr14:49806260 | T | A | 45 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0041 others(42): Show |
45 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1745-127A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806260 | |||||||
| chr14:49806261 | T | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(84): Show |
87 | HG00323.hp2 HG00558.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.1745-128A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806261 | |||||||
| chr14:49806262 | T | A | 39 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0041 others(36): Show |
39 | HG00558.hp2 HG00639.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1745-129A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806262 | |||||||
| chr14:49806263 | T | A | 52 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(49): Show |
52 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.1745-130A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806263 | |||||||
| chr14:49806264 | T | A | 19 | a0001c0001t0001g0039 a0001c0001t0001g0047 a0001c0001t0001g0050 others(16): Show |
19 | HG01074.hp1 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1745-131A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806264 | |||||||
| chr14:49806265 | T | A | 18 | a0001c0001t0001g0015 a0001c0001t0001g0046 a0001c0001t0001g0058 others(15): Show |
18 | HG01169.hp1 HG01169.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1745-132A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806265 | |||||||
| chr14:49806266 | T | A | 8 | a0001c0001t0001g0047 a0001c0001t0001g0079 a0001c0001t0001g0102 others(5): Show |
8 | HG01074.hp1 HG01074.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.1745-133A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806266 | |||||||
| chr14:49806267 | T | A | 9 | a0001c0001t0001g0046 a0001c0001t0001g0058 a0001c0001t0001g0061 others(6): Show |
9 | HG01169.hp2 HG02109.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.1745-134A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806267 | |||||||
| chr14:49806268 | T | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0102 |
2 | HG02602.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1745-135A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806268 | |||||||
| chr14:49806269 | T | A | 2 | a0001c0001t0001g0161 a0001c0001t0002g0012 |
2 | HG02109.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1745-136A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806269 | |||||||
| chr14:49806325 | A | G | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1745-192T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806325 | |||||||
| chr14:49806496 | A | G | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1745-363T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806496 | |||||||
| chr14:49806541 | T | C | 3 | a0001c0001t0001g0015 a0001c0001t0002g0014 a0001c0004t0002g0016 |
3 | HG02615.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1745-408A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806541 | |||||||
| chr14:49806645 | ACTC | A | 55 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0018 others(52): Show |
55 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.1745-515_1745-513d others(5): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806645 | |||||||
| chr14:49806680 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1745-547G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49806680 | |||||||
| chr14:49807290 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1745-1157A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49807290 | |||||||
| chr14:49807392 | ATATACC | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0079 |
2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1745-1265_1745-126 others(10): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49807392 | |||||||
| chr14:49807400 | A | G | 2 | a0001c0001t0001g0064 a0001c0001t0001g0079 |
2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1745-1267T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49807400 | |||||||
| chr14:49807473 | T | A | 1 | a0002c0003t0010g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1745-1340A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49807473 | |||||||
| chr14:49807561 | CAT | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1745-1430_1745-142 others(6): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49807561 | |||||||
| chr14:49807592 | A | AT | 11 | a0001c0001t0001g0060 a0001c0001t0001g0109 a0001c0001t0001g0110 others(8): Show |
11 | HG00642.hp1 HG01255.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1745-1460dupA | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49807592 | |||||||
| chr14:49807592 | AT | A | 9 | a0001c0001t0001g0081 a0001c0001t0001g0096 a0001c0001t0001g0103 others(6): Show |
9 | HG00609.hp1 HG00609.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.1745-1460delA | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49807592 | |||||||
| chr14:49807655 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1745-1522C>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49807655 | |||||||
| chr14:49807792 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1745-1659A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49807792 | |||||||
| chr14:49807984 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1745-1851C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49807984 | |||||||
| chr14:49808076 | C | G | 1 | a0001c0001t0003g0187 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1745-1943G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49808076 | |||||||
| chr14:49808194 | G | C | 2 | a0002c0003t0004g0216 a0002c0003t0004g0221 |
2 | HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1745-2061C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49808194 | |||||||
| chr14:49808205 | G | T | 169 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(166): Show |
169 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.1745-2072C>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49808205 | |||||||
| chr14:49808317 | C | T | 1 | a0001c0001t0003g0180 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1745-2184G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49808317 | |||||||
| chr14:49808318 | A | G | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1745-2185T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49808318 | |||||||
| chr14:49808320 | C | A | 1 | a0002c0003t0010g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1745-2187G>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49808320 | |||||||
| chr14:49808701 | C | T | 1 | a0002c0003t0010g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1745-2568G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49808701 | |||||||
| chr14:49808891 | G | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1745-2758C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49808891 | |||||||
| chr14:49808923 | T | C | 1 | a0001c0001t0003g0187 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1745-2790A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49808923 | |||||||
| chr14:49809105 | A | G | 12 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(9): Show |
12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1745-2972T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49809105 | |||||||
| chr14:49809557 | C | CTATA | 7 | a0001c0001t0001g0033 a0001c0001t0002g0031 a0001c0004t0002g0032 others(4): Show |
7 | HG02559.hp2 HG02886.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1745-3428_1745-342 others(8): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49809557 | |||||||
| chr14:49809574 | G | C | 1 | a0001c0001t0001g0059 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1745-3441C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49809574 | |||||||
| chr14:49809639 | G | C | 8 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1745-3506C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49809639 | |||||||
| chr14:49809721 | G | A | 8 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1745-3588C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49809721 | |||||||
| chr14:49809734 | C | A | 2 | a0001c0001t0001g0015 a0001c0001t0002g0014 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1745-3601G>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49809734 | |||||||
| chr14:49809904 | C | T | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.1745-3771G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49809904 | |||||||
| chr14:49809949 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1745-3816G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49809949 | |||||||
| chr14:49809950 | G | A | 1 | a0002c0003t0004g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1745-3817C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49809950 | |||||||
| chr14:49809986 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1745-3853C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49809986 | |||||||
| chr14:49810104 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02109.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1744+3884G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49810104 | |||||||
| chr14:49810140 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1744+3848C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49810140 | |||||||
| chr14:49810161 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1744+3827C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49810161 | |||||||
| chr14:49810361 | C | T | 8 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1744+3627G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49810361 | |||||||
| chr14:49810364 | C | T | 1 | a0001c0001t0003g0195 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1744+3624G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49810364 | |||||||
| chr14:49810564 | C | T | 1 | a0002c0003t0010g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1744+3424G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49810564 | |||||||
| chr14:49810620 | T | G | 1 | a0001c0001t0001g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1744+3368A>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49810620 | |||||||
| chr14:49810653 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1744+3335A>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49810653 | |||||||
| chr14:49810820 | A | G | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1744+3168T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49810820 | |||||||
| chr14:49810906 | G | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 |
3 | HG01952.hp2 HG01993.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1744+3082C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49810906 | |||||||
| chr14:49811071 | T | C | 8 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1744+2917A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49811071 | |||||||
| chr14:49811130 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1744+2858T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49811130 | |||||||
| chr14:49811157 | C | T | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.1744+2831G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49811157 | |||||||
| chr14:49811228 | T | C | 7 | a0001c0001t0001g0033 a0001c0001t0002g0031 a0001c0004t0002g0032 others(4): Show |
7 | HG02559.hp2 HG02886.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1744+2760A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49811228 | |||||||
| chr14:49811426 | AT | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1744+2561delA | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49811426 | |||||||
| chr14:49811707 | T | C | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(164): Show |
167 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1744+2281A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49811707 | |||||||
| chr14:49811729 | T | C | 25 | a0001c0001t0003g0001 a0001c0001t0003g0176 a0001c0001t0003g0177 others(22): Show |
26 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1744+2259A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49811729 | |||||||
| chr14:49811766 | G | A | 1 | a0001c0011t0001g0083 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1744+2222C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49811766 | |||||||
| chr14:49812063 | T | A | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.1744+1925A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49812063 | |||||||
| chr14:49812252 | G | A | 8 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1744+1736C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49812252 | |||||||
| chr14:49812447 | C | T | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.1744+1541G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49812447 | |||||||
| chr14:49812629 | G | A | 1 | a0001c0001t0002g0168 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1744+1359C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49812629 | |||||||
| chr14:49812678 | T | G | 1 | a0001c0001t0001g0002 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1744+1310A>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49812678 | |||||||
| chr14:49813074 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(195): Show |
199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1744+914G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49813074 | |||||||
| chr14:49813241 | A | C | 25 | a0001c0001t0003g0001 a0001c0001t0003g0176 a0001c0001t0003g0177 others(22): Show |
26 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1744+747T>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49813241 | |||||||
| chr14:49813247 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1744+741C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49813247 | |||||||
| chr14:49813482 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1744+506A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49813482 | |||||||
| chr14:49813554 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1744+434C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49813554 | |||||||
| chr14:49813624 | T | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1744+364A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49813624 | |||||||
| chr14:49813639 | T | C | 2 | a0001c0001t0001g0063 a0001c0005t0001g0140 |
2 | HG01496.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1744+349A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49813639 | |||||||
| chr14:49813647 | C | T | 1 | a0002c0003t0010g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1744+341G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49813647 | |||||||
| chr14:49813662 | G | GGTGTGTG others(1): Show |
8 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1744+318_1744+325d others(10): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49813662 | |||||||
| chr14:49813662 | GGTGT | G | 10 | a0001c0001t0001g0061 a0001c0001t0001g0087 a0001c0001t0002g0084 others(7): Show |
10 | HG00597.hp2 HG01074.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.1744+322_1744+325d others(6): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49813662 | |||||||
| chr14:49813780 | T | A | 8 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1744+208A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49813780 | |||||||
| chr14:49813858 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0002g0117 |
2 | HG01361.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1744+130G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49813858 | |||||||
| chr14:49813859 | T | C | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(215): Show |
219 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.1744+129A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49813859 | |||||||
| chr14:49813894 | A | C | 1 | a0001c0001t0002g0167 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1744+94T>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49813894 | |||||||
| chr14:49813970 | T | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(191): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1744+18A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | 49813970 | |||||||
| chr14:49814156 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02109.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1682-106C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 17/32 | chr14 | 49814156 | |||||||
| chr14:49814198 | C | T | 1 | a0001c0001t0009g0013 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1682-148G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 17/32 | chr14 | 49814198 | |||||||
| chr14:49814241 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1682-191T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 17/32 | chr14 | 49814241 | |||||||
| chr14:49814615 | A | T | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.1681+139T>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 17/32 | chr14 | 49814615 | |||||||
| chr14:49814949 | AAG | A | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.1578-94_1578-93del others(2): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49814949 | |||||||
| chr14:49815004 | C | T | 4 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0023 others(1): Show |
4 | HG01081.hp2 HG01175.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1578-147G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49815004 | |||||||
| chr14:49815072 | TA | T | 4 | a0001c0001t0001g0101 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
4 | HG02622.hp2 HG03041.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1578-216delT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49815072 | |||||||
| chr14:49815261 | C | G | 1 | a0001c0001t0002g0021 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1578-404G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49815261 | |||||||
| chr14:49815740 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1578-883C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49815740 | |||||||
| chr14:49815778 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1578-921G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49815778 | |||||||
| chr14:49815788 | A | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1578-931T>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49815788 | |||||||
| chr14:49815800 | T | C | 2 | a0001c0001t0001g0051 a0001c0001t0001g0093 |
2 | HG02080.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1578-943A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49815800 | |||||||
| chr14:49816503 | G | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1578-1646C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49816503 | |||||||
| chr14:49816639 | A | G | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.1578-1782T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49816639 | |||||||
| chr14:49816817 | A | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(191): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1578-1960T>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49816817 | |||||||
| chr14:49816878 | G | A | 1 | a0002c0003t0004g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1578-2021C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49816878 | |||||||
| chr14:49817126 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1578-2269T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49817126 | |||||||
| chr14:49817419 | G | C | 1 | a0001c0001t0006g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1578-2562C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49817419 | |||||||
| chr14:49817485 | C | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(191): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1578-2628G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49817485 | |||||||
| chr14:49817503 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1578-2646T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49817503 | |||||||
| chr14:49817963 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(191): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1578-3106T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49817963 | |||||||
| chr14:49818071 | A | G | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.1578-3214T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49818071 | |||||||
| chr14:49818084 | C | CT | 17 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0107 others(14): Show |
17 | HG00597.hp2 HG00735.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1578-3228dupA | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49818084 | |||||||
| chr14:49818084 | CT | C | 11 | a0001c0001t0001g0115 a0001c0001t0003g0177 a0001c0001t0003g0178 others(8): Show |
11 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1578-3228delA | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49818084 | |||||||
| chr14:49818123 | T | C | 44 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0033 others(41): Show |
44 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.1578-3266A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49818123 | |||||||
| chr14:49818173 | C | T | 170 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(167): Show |
170 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.1578-3316G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49818173 | |||||||
| chr14:49818230 | A | G | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.1578-3373T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49818230 | |||||||
| chr14:49818371 | C | T | 1 | a0002c0002t0001g0137 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1578-3514G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49818371 | |||||||
| chr14:49818384 | G | A | 6 | a0001c0001t0001g0052 a0001c0001t0001g0090 a0001c0001t0001g0091 others(3): Show |
6 | HG02056.hp1 HG02056.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.1578-3527C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49818384 | |||||||
| chr14:49818636 | C | T | 1 | a0001c0001t0002g0089 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1578-3779G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49818636 | |||||||
| chr14:49818781 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1578-3924G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49818781 | |||||||
| chr14:49818893 | C | T | 8 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1578-4036G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49818893 | |||||||
| chr14:49818963 | C | A | 8 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1578-4106G>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49818963 | |||||||
| chr14:49819095 | G | A | 24 | a0001c0001t0001g0003 a0001c0001t0001g0155 a0001c0001t0002g0010 others(21): Show |
24 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.1578-4238C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49819095 | |||||||
| chr14:49819148 | T | C | 2 | a0001c0004t0002g0034 a0001c0004t0002g0035 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1578-4291A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49819148 | |||||||
| chr14:49819313 | G | C | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.1578-4456C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49819313 | |||||||
| chr14:49819384 | T | C | 12 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(9): Show |
12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1578-4527A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49819384 | |||||||
| chr14:49819392 | CAT | C | 11 | a0002c0003t0004g0210 a0002c0003t0004g0211 a0002c0003t0004g0212 others(8): Show |
11 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1578-4537_1578-453 others(6): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49819392 | |||||||
| chr14:49819392 | CATATAT | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0062 others(19): Show |
22 | HG00673.hp1 HG01069.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.1578-4541_1578-453 others(10): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49819392 | |||||||
| chr14:49819392 | CATATATA others(1): Show |
C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(169): Show |
173 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.1578-4543_1578-453 others(12): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49819392 | |||||||
| chr14:49819392 | CATATATA others(3): Show |
C | 12 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0003g0177 others(9): Show |
12 | HG00642.hp1 HG01168.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1578-4545_1578-453 others(14): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49819392 | |||||||
| chr14:49819410 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1578-4553A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49819410 | |||||||
| chr14:49819697 | G | T | 1 | a0001c0001t0001g0061 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1578-4840C>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49819697 | |||||||
| chr14:49819737 | T | C | 1 | a0002c0003t0010g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1578-4880A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49819737 | |||||||
| chr14:49819883 | T | C | 1 | a0001c0004t0002g0016 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1578-5026A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49819883 | |||||||
| chr14:49819950 | T | G | 2 | a0001c0001t0001g0134 a0002c0003t0010g0175 |
2 | HG01993.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1578-5093A>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49819950 | |||||||
| chr14:49819962 | T | A | 13 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0003g0177 others(10): Show |
13 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.1578-5105A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49819962 | |||||||
| chr14:49820096 | C | G | 1 | a0002c0003t0004g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1578-5239G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49820096 | |||||||
| chr14:49820097 | A | G | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 |
3 | HG01952.hp2 HG01993.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1578-5240T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49820097 | |||||||
| chr14:49820141 | G | C | 5 | a0001c0001t0002g0080 a0001c0001t0002g0139 a0001c0001t0002g0165 others(2): Show |
5 | HG00544.hp1 HG00621.hp2 HG00673.hp2 others(2): Show |
intron_variant | MODIFIER | c.1578-5284C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49820141 | |||||||
| chr14:49820466 | T | C | 1 | a0001c0009t0001g0092 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1577+5401A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49820466 | |||||||
| chr14:49820499 | T | G | 1 | a0001c0001t0002g0112 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1577+5368A>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49820499 | |||||||
| chr14:49820610 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(191): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1577+5257C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49820610 | |||||||
| chr14:49820742 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1577+5125G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49820742 | |||||||
| chr14:49820746 | T | G | 8 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1577+5121A>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49820746 | |||||||
| chr14:49820774 | C | T | 12 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(9): Show |
12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1577+5093G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49820774 | |||||||
| chr14:49820974 | AGTGAGGA others(521): Show |
A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(191): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1577+4365_1577+489 others(4): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49820974 | |||||||
| chr14:49821013 | T | C | 12 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(9): Show |
12 | HG00597.hp2 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1577+4854A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49821013 | |||||||
| chr14:49821100 | G | A | 1 | a0002c0003t0010g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1577+4767C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49821100 | |||||||
| chr14:49821213 | TG | T | 12 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(9): Show |
12 | HG00597.hp2 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1577+4653delC | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49821213 | |||||||
| chr14:49821268 | C | CTCAGCCC others(43): Show |
1 | a0002c0002t0005g0005 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1577+4549_1577+459 others(54): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49821268 | |||||||
| chr14:49821310 | T | TGGGGGGG others(44): Show |
3 | a0002c0002t0005g0004 a0002c0002t0005g0006 a0002c0002t0005g0007 |
3 | HG00597.hp2 NA19011.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1577+4506_1577+455 others(55): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49821310 | |||||||
| chr14:49821346 | G | A | 1 | a0002c0003t0010g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1577+4521C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49821346 | |||||||
| chr14:49821592 | GGTCAGCC others(43): Show |
G | 1 | a0001c0001t0001g0143 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1577+4225_1577+427 others(54): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49821592 | |||||||
| chr14:49821604 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1577+4263C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49821604 | |||||||
| chr14:49821625 | G | A | 1 | a0002c0003t0010g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1577+4242C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49821625 | |||||||
| chr14:49821641 | GC | G | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(202): Show |
206 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.1577+4225delG | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49821641 | |||||||
| chr14:49821664 | C | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1577+4203G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49821664 | |||||||
| chr14:49821724 | G | A | 10 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0200 others(7): Show |
10 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1577+4143C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49821724 | |||||||
| chr14:49821778 | C | G | 1 | a0001c0011t0001g0083 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1577+4089G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49821778 | |||||||
| chr14:49821807 | G | A | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(164): Show |
167 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1577+4060C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49821807 | |||||||
| chr14:49821830 | T | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1577+4037A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49821830 | |||||||
| chr14:49821949 | A | G | 1 | a0001c0011t0001g0083 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1577+3918T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49821949 | |||||||
| chr14:49822143 | A | G | 1 | a0002c0003t0010g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1577+3724T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49822143 | |||||||
| chr14:49822291 | AAAAAT | A | 23 | a0001c0001t0003g0001 a0001c0001t0003g0176 a0001c0001t0003g0179 others(20): Show |
24 | HG00280.hp1 HG00639.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1577+3571_1577+357 others(9): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49822291 | |||||||
| chr14:49822319 | A | T | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(189): Show |
193 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1577+3548T>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49822319 | |||||||
| chr14:49822335 | T | A | 1 | a0001c0011t0001g0083 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1577+3532A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49822335 | |||||||
| chr14:49822452 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1577+3415A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49822452 | |||||||
| chr14:49822499 | C | T | 169 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(166): Show |
169 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.1577+3368G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49822499 | |||||||
| chr14:49822536 | T | G | 1 | a0001c0001t0001g0145 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1577+3331A>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49822536 | |||||||
| chr14:49822581 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1577+3286C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49822581 | |||||||
| chr14:49822638 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1577+3229A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49822638 | |||||||
| chr14:49822658 | A | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1577+3209T>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49822658 | |||||||
| chr14:49822659 | G | A | 1 | a0002c0002t0001g0202 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1577+3208C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49822659 | |||||||
| chr14:49822668 | TAA | T | 26 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0001t0001g0052 others(23): Show |
26 | HG00544.hp2 HG01074.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.1577+3197_1577+319 others(6): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49822668 | |||||||
| chr14:49822668 | TAAAA | T | 11 | a0001c0001t0001g0044 a0001c0001t0001g0059 a0001c0001t0002g0029 others(8): Show |
11 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(8): Show |
intron_variant | MODIFIER | c.1577+3195_1577+319 others(8): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49822668 | |||||||
| chr14:49822757 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1577+3110A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49822757 | |||||||
| chr14:49822766 | G | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(189): Show |
193 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1577+3101C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49822766 | |||||||
| chr14:49822800 | G | A | 10 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0200 others(7): Show |
10 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1577+3067C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49822800 | |||||||
| chr14:49822810 | G | T | 1 | a0001c0001t0002g0019 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1577+3057C>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49822810 | |||||||
| chr14:49822843 | C | G | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0098 others(1): Show |
4 | HG02056.hp1 HG02080.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1577+3024G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49822843 | |||||||
| chr14:49822867 | T | C | 2 | a0001c0001t0002g0026 a0001c0001t0002g0027 |
2 | HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1577+3000A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49822867 | |||||||
| chr14:49822934 | AT | A | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(197): Show |
201 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.1577+2932delA | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49822934 | |||||||
| chr14:49823005 | C | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1577+2862G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49823005 | |||||||
| chr14:49823171 | C | A | 12 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(9): Show |
12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1577+2696G>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49823171 | |||||||
| chr14:49823198 | C | A | 23 | a0001c0001t0001g0155 a0001c0001t0002g0010 a0001c0001t0002g0011 others(20): Show |
23 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1577+2669G>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49823198 | |||||||
| chr14:49823462 | G | A | 1 | a0001c0001t0003g0192 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1577+2405C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49823462 | |||||||
| chr14:49823786 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1577+2081A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49823786 | |||||||
| chr14:49823853 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1577+2014C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49823853 | |||||||
| chr14:49823935 | G | C | 23 | a0001c0001t0001g0155 a0001c0001t0002g0010 a0001c0001t0002g0011 others(20): Show |
23 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1577+1932C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49823935 | |||||||
| chr14:49824100 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1577+1767C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49824100 | |||||||
| chr14:49824544 | C | CA | 17 | a0001c0001t0001g0046 a0001c0001t0001g0053 a0001c0001t0001g0130 others(14): Show |
17 | HG00280.hp2 HG00597.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1577+1322dupT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49824544 | |||||||
| chr14:49824544 | C | CAA | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(182): Show |
186 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1577+1321_1577+132 others(6): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49824544 | |||||||
| chr14:49824599 | A | C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1577+1268T>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49824599 | |||||||
| chr14:49824912 | G | A | 1 | a0002c0003t0004g0216 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1577+955C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49824912 | |||||||
| chr14:49824939 | T | A | 11 | a0001c0001t0003g0177 a0001c0001t0003g0178 a0001c0001t0003g0184 others(8): Show |
11 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1577+928A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49824939 | |||||||
| chr14:49825474 | C | T | 12 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(9): Show |
12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1577+393G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49825474 | |||||||
| chr14:49825542 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1577+325G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 16/32 | chr14 | 49825542 | |||||||
| chr14:49826064 | C | G | 1 | a0001c0001t0002g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1489-109G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49826064 | |||||||
| chr14:49826081 | A | AAC | 6 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0077 others(3): Show |
6 | HG00280.hp1 HG00597.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.1489-128_1489-127d others(4): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49826081 | |||||||
| chr14:49826172 | T | G | 1 | a0002c0003t0004g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1489-217A>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49826172 | |||||||
| chr14:49826462 | G | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(203): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1489-507C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49826462 | |||||||
| chr14:49826540 | CA | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(196): Show |
200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.1489-586delT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49826540 | |||||||
| chr14:49826540 | CAA | C | 8 | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0123 others(5): Show |
8 | HG00280.hp2 HG00544.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.1489-587_1489-586d others(4): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49826540 | |||||||
| chr14:49826576 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1489-621G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49826576 | |||||||
| chr14:49826626 | C | T | 1 | a0002c0003t0010g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1489-671G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49826626 | |||||||
| chr14:49826648 | C | G | 12 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(9): Show |
12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1489-693G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49826648 | |||||||
| chr14:49826850 | C | G | 10 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0200 others(7): Show |
10 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1489-895G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49826850 | |||||||
| chr14:49826962 | G | A | 4 | a0001c0001t0003g0177 a0001c0001t0003g0178 a0001c0001t0003g0184 others(1): Show |
4 | HG00642.hp1 HG01168.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1489-1007C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49826962 | |||||||
| chr14:49827042 | A | G | 14 | a0001c0001t0001g0033 a0001c0001t0002g0019 a0001c0001t0002g0026 others(11): Show |
14 | HG01891.hp1 HG02559.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.1489-1087T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49827042 | |||||||
| chr14:49827043 | A | T | 14 | a0001c0001t0001g0033 a0001c0001t0002g0019 a0001c0001t0002g0026 others(11): Show |
14 | HG01891.hp1 HG02559.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.1489-1088T>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49827043 | |||||||
| chr14:49827131 | T | C | 1 | a0001c0001t0001g0009 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1488+1160A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49827131 | |||||||
| chr14:49827271 | C | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1488+1020G>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49827271 | |||||||
| chr14:49827336 | G | A | 1 | a0001c0001t0003g0184 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1488+955C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49827336 | |||||||
| chr14:49827433 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1488+858C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49827433 | |||||||
| chr14:49827676 | G | A | 3 | a0001c0001t0001g0081 a0001c0001t0001g0095 a0001c0001t0001g0096 |
3 | HG01433.hp2 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1488+615C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49827676 | |||||||
| chr14:49827728 | G | A | 3 | a0001c0001t0001g0105 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | HG01069.hp2 HG01255.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1488+563C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49827728 | |||||||
| chr14:49827813 | C | CA | 7 | a0001c0001t0001g0171 a0002c0002t0001g0200 a0002c0002t0001g0201 others(4): Show |
7 | HG02257.hp1 HG02451.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1488+477dupT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49827813 | |||||||
| chr14:49827880 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1488+411C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49827880 | |||||||
| chr14:49828018 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1488+273A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49828018 | |||||||
| chr14:49828026 | T | C | 1 | a0002c0002t0001g0203 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1488+265A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49828026 | |||||||
| chr14:49828185 | A | G | 1 | a0001c0001t0003g0195 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1488+106T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 15/32 | chr14 | 49828185 | |||||||
| chr14:49828443 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1425-89A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 14/32 | chr14 | 49828443 | |||||||
| chr14:49828540 | A | T | 1 | a0001c0001t0001g0129 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1424+76T>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 14/32 | chr14 | 49828540 | |||||||
| chr14:49828557 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1424+59A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 14/32 | chr14 | 49828557 | |||||||
| chr14:49828899 | A | G | 6 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(3): Show |
6 | HG00609.hp1 HG02135.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1233-92T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 13/32 | chr14 | 49828899 | |||||||
| chr14:49829300 | G | A | 1 | a0002c0002t0001g0137 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1024-38C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 12/32 | chr14 | 49829300 | |||||||
| chr14:49829520 | T | C | 1 | a0001c0001t0003g0176 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.946-94A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 11/32 | chr14 | 49829520 | |||||||
| chr14:49829746 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.946-320T>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 11/32 | chr14 | 49829746 | |||||||
| chr14:49829911 | G | T | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.946-485C>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 11/32 | chr14 | 49829911 | |||||||
| chr14:49830388 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.945+911T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 11/32 | chr14 | 49830388 | |||||||
| chr14:49830557 | G | T | 1 | a0001c0001t0003g0185 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.945+742C>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 11/32 | chr14 | 49830557 | |||||||
| chr14:49830744 | C | T | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(204): Show |
208 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.945+555G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 11/32 | chr14 | 49830744 | |||||||
| chr14:49830931 | T | C | 1 | a0001c0010t0002g0169 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.945+368A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 11/32 | chr14 | 49830931 | |||||||
| chr14:49831020 | C | A | 12 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(9): Show |
12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.945+279G>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 11/32 | chr14 | 49831020 | |||||||
| chr14:49831049 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.945+250G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 11/32 | chr14 | 49831049 | |||||||
| chr14:49831080 | A | G | 12 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(9): Show |
12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.945+219T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 11/32 | chr14 | 49831080 | |||||||
| chr14:49831382 | C | G | 1 | a0001c0001t0001g0045 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.883-21G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 10/32 | chr14 | 49831382 | |||||||
| chr14:49831435 | A | C | 12 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(9): Show |
12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.883-74T>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 10/32 | chr14 | 49831435 | |||||||
| chr14:49831435 | AT | A | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(164): Show |
167 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.883-75delA | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 10/32 | chr14 | 49831435 | |||||||
| chr14:49831530 | G | T | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(204): Show |
208 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.883-169C>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 10/32 | chr14 | 49831530 | |||||||
| chr14:49831668 | C | A | 12 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(9): Show |
12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.883-307G>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 10/32 | chr14 | 49831668 | |||||||
| chr14:49831675 | G | C | 10 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0200 others(7): Show |
10 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.883-314C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 10/32 | chr14 | 49831675 | |||||||
| chr14:49831880 | G | C | 2 | a0001c0001t0001g0171 a0001c0011t0001g0083 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.882+171C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 10/32 | chr14 | 49831880 | |||||||
| chr14:49832169 | A | G | 10 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0200 others(7): Show |
10 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.806+38T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 9/32 | chr14 | 49832169 | |||||||
| chr14:49832576 | G | A | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.736-299C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 8/32 | chr14 | 49832576 | |||||||
| chr14:49832761 | A | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(204): Show |
208 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.736-484T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 8/32 | chr14 | 49832761 | |||||||
| chr14:49832914 | T | C | 25 | a0001c0001t0003g0001 a0001c0001t0003g0176 a0001c0001t0003g0177 others(22): Show |
26 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.735+509A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 8/32 | chr14 | 49832914 | |||||||
| chr14:49832953 | A | G | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.735+470T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 8/32 | chr14 | 49832953 | |||||||
| chr14:49833076 | G | A | 1 | a0001c0001t0006g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.735+347C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 8/32 | chr14 | 49833076 | |||||||
| chr14:49833351 | C | T | 1 | a0002c0003t0010g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.735+72G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 8/32 | chr14 | 49833351 | |||||||
| chr14:49833510 | A | G | 1 | a0003c0008t0001g0142 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.662-14T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 7/32 | chr14 | 49833510 | |||||||
| chr14:49833592 | A | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(204): Show |
208 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.662-96T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 7/32 | chr14 | 49833592 | |||||||
| chr14:49833601 | T | C | 1 | a0002c0003t0010g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.662-105A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 7/32 | chr14 | 49833601 | |||||||
| chr14:49833762 | A | G | 6 | a0002c0003t0004g0215 a0002c0003t0004g0216 a0002c0003t0004g0218 others(3): Show |
6 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.662-266T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 7/32 | chr14 | 49833762 | |||||||
| chr14:49833882 | T | A | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-386A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 7/32 | chr14 | 49833882 | |||||||
| chr14:49833917 | A | G | 1 | a0001c0001t0002g0112 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.662-421T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 7/32 | chr14 | 49833917 | |||||||
| chr14:49834637 | C | G | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.575-188G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49834637 | |||||||
| chr14:49834810 | C | A | 9 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(6): Show |
9 | HG01069.hp1 HG01123.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.575-361G>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49834810 | |||||||
| chr14:49835131 | C | A | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.575-682G>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49835131 | |||||||
| chr14:49835195 | C | T | 1 | a0002c0003t0010g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.575-746G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49835195 | |||||||
| chr14:49835218 | C | CA | 191 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(188): Show |
192 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.575-770dupT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49835218 | |||||||
| chr14:49835218 | C | CAA | 9 | a0001c0001t0001g0053 a0001c0001t0001g0087 a0001c0001t0001g0096 others(6): Show |
9 | HG00738.hp2 HG00741.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.575-771_575-770dup others(2): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49835218 | |||||||
| chr14:49835218 | CA | C | 12 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(9): Show |
12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.575-770delT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49835218 | |||||||
| chr14:49835748 | C | T | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(204): Show |
208 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.575-1299G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49835748 | |||||||
| chr14:49835877 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(191): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.575-1428T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49835877 | |||||||
| chr14:49835987 | T | A | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.575-1538A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49835987 | |||||||
| chr14:49836182 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.575-1733C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49836182 | |||||||
| chr14:49836374 | G | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG02622.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.574+1765C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49836374 | |||||||
| chr14:49836496 | T | C | 10 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0200 others(7): Show |
10 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.574+1643A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49836496 | |||||||
| chr14:49836562 | C | T | 11 | a0002c0003t0004g0210 a0002c0003t0004g0211 a0002c0003t0004g0212 others(8): Show |
11 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.574+1577G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49836562 | |||||||
| chr14:49836763 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.574+1376A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49836763 | |||||||
| chr14:49836868 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.574+1271G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49836868 | |||||||
| chr14:49837137 | G | A | 2 | a0001c0001t0003g0181 a0001c0001t0003g0182 |
2 | HG00738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.574+1002C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49837137 | |||||||
| chr14:49837334 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.574+805G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49837334 | |||||||
| chr14:49837626 | T | C | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(164): Show |
167 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.574+513A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49837626 | |||||||
| chr14:49837764 | T | C | 6 | a0001c0001t0001g0052 a0001c0001t0001g0090 a0001c0001t0001g0091 others(3): Show |
6 | HG02056.hp1 HG02056.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.574+375A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49837764 | |||||||
| chr14:49837815 | T | TA | 13 | a0001c0001t0003g0176 a0001c0001t0003g0192 a0002c0002t0001g0137 others(10): Show |
13 | HG01978.hp1 HG02145.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.574+323dupT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49837815 | |||||||
| chr14:49837815 | TA | T | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(159): Show |
162 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.574+323delT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49837815 | |||||||
| chr14:49837835 | C | A | 1 | a0002c0002t0001g0204 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.574+304G>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49837835 | |||||||
| chr14:49837978 | A | T | 1 | a0001c0001t0001g0106 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.574+161T>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49837978 | |||||||
| chr14:49838100 | C | G | 1 | a0001c0001t0003g0197 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.574+39G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 6/32 | chr14 | 49838100 | |||||||
| chr14:49838261 | T | A | 1 | a0001c0001t0003g0182 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.507-55A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49838261 | |||||||
| chr14:49838369 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.507-163T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49838369 | |||||||
| chr14:49838435 | C | T | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(164): Show |
167 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.507-229G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49838435 | |||||||
| chr14:49838524 | C | T | 24 | a0001c0001t0003g0001 a0001c0001t0003g0176 a0001c0001t0003g0177 others(21): Show |
25 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.507-318G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49838524 | |||||||
| chr14:49838525 | A | T | 8 | a0001c0001t0001g0033 a0001c0001t0002g0030 a0001c0001t0002g0031 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.507-319T>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49838525 | |||||||
| chr14:49838585 | G | GT | 10 | a0001c0001t0001g0015 a0001c0001t0001g0041 a0001c0001t0001g0057 others(7): Show |
10 | HG00735.hp1 HG01175.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.507-380dupA | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49838585 | |||||||
| chr14:49838585 | GT | G | 7 | a0001c0001t0001g0109 a0001c0001t0001g0127 a0001c0001t0001g0161 others(4): Show |
7 | HG01168.hp2 HG01257.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.507-380delA | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49838585 | |||||||
| chr14:49838648 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.507-442C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49838648 | |||||||
| chr14:49838713 | T | C | 27 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0003g0001 others(24): Show |
28 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.507-507A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49838713 | |||||||
| chr14:49838714 | A | G | 1 | a0001c0001t0002g0019 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.507-508T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49838714 | |||||||
| chr14:49838718 | A | G | 25 | a0001c0001t0003g0001 a0001c0001t0003g0176 a0001c0001t0003g0177 others(22): Show |
26 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.507-512T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49838718 | |||||||
| chr14:49838729 | C | A | 1 | a0001c0001t0002g0168 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.507-523G>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49838729 | |||||||
| chr14:49838729 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.507-523G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49838729 | |||||||
| chr14:49838786 | G | A | 1 | a0001c0001t0007g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.507-580C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49838786 | |||||||
| chr14:49838806 | A | G | 1 | a0001c0001t0007g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.507-600T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49838806 | |||||||
| chr14:49838858 | A | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0159 |
3 | HG00621.hp1 HG02004.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.507-652T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49838858 | |||||||
| chr14:49838862 | G | A | 8 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(5): Show |
8 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.507-656C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49838862 | |||||||
| chr14:49838903 | C | G | 20 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0200 others(17): Show |
20 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.507-697G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49838903 | |||||||
| chr14:49838914 | A | C | 2 | a0001c0001t0003g0177 a0001c0001t0003g0178 |
2 | HG00642.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.507-708T>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49838914 | |||||||
| chr14:49839067 | A | AT | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(160): Show |
164 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.507-862dupA | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49839067 | |||||||
| chr14:49839081 | A | T | 1 | a0001c0001t0003g0192 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.507-875T>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49839081 | |||||||
| chr14:49839273 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.507-1067C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49839273 | |||||||
| chr14:49839383 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.507-1177G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49839383 | |||||||
| chr14:49840227 | C | T | 1 | a0001c0001t0003g0194 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.506+491G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49840227 | |||||||
| chr14:49840240 | T | C | 1 | a0001c0004t0002g0016 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.506+478A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49840240 | |||||||
| chr14:49840244 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0002g0117 |
2 | HG01361.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.506+474G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49840244 | |||||||
| chr14:49840355 | G | A | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(204): Show |
208 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.506+363C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49840355 | |||||||
| chr14:49840364 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.506+354G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49840364 | |||||||
| chr14:49840461 | C | CA | 12 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(9): Show |
12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.506+256dupT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49840461 | |||||||
| chr14:49840461 | CA | C | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(201): Show |
205 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.506+256delT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49840461 | |||||||
| chr14:49840619 | A | G | 1 | a0001c0001t0003g0184 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.506+99T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49840619 | |||||||
| chr14:49840688 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.506+30G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 5/32 | chr14 | 49840688 | |||||||
| chr14:49840873 | T | C | 8 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.358-7A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49840873 | |||||||
| chr14:49840997 | G | A | 1 | a0002c0002t0001g0138 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.358-131C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49840997 | |||||||
| chr14:49841046 | A | G | 1 | a0001c0001t0003g0183 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.358-180T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49841046 | |||||||
| chr14:49841094 | G | T | 1 | a0002c0003t0010g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.358-228C>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49841094 | |||||||
| chr14:49841196 | C | CA | 10 | a0001c0001t0001g0116 a0002c0002t0001g0200 a0002c0002t0001g0201 others(7): Show |
10 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.358-331dupT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49841196 | |||||||
| chr14:49841196 | C | CAA | 10 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(7): Show |
10 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.358-332_358-331dup others(2): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49841196 | |||||||
| chr14:49841196 | CA | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(161): Show |
165 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.358-331delT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49841196 | |||||||
| chr14:49841223 | T | TA | 12 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(9): Show |
12 | HG00597.hp2 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.358-358dupT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49841223 | |||||||
| chr14:49841262 | ATT | A | 8 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.358-398_358-397del others(2): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49841262 | |||||||
| chr14:49841340 | C | G | 1 | a0001c0001t0001g0055 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.358-474G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49841340 | |||||||
| chr14:49841345 | A | C | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(204): Show |
208 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.358-479T>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49841345 | |||||||
| chr14:49841435 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.358-569C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49841435 | |||||||
| chr14:49841578 | G | GA | 27 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0086 others(24): Show |
28 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.358-713dupT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49841578 | |||||||
| chr14:49841578 | G | GAA | 5 | a0001c0001t0003g0181 a0001c0001t0003g0182 a0001c0001t0003g0191 others(2): Show |
5 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.358-714_358-713dup others(2): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49841578 | |||||||
| chr14:49841578 | GA | G | 9 | a0001c0001t0001g0054 a0001c0001t0001g0123 a0001c0001t0001g0128 others(6): Show |
9 | HG00597.hp2 HG01123.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.358-713delT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49841578 | |||||||
| chr14:49841578 | GAA | G | 7 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(4): Show |
7 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.358-714_358-713del others(2): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49841578 | |||||||
| chr14:49841696 | T | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(197): Show |
201 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.358-830A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49841696 | |||||||
| chr14:49842143 | G | GA | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(193): Show |
197 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.358-1278dupT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49842143 | |||||||
| chr14:49842226 | A | AG | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(191): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.358-1361dupC | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49842226 | |||||||
| chr14:49842228 | G | A | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-1362C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49842228 | |||||||
| chr14:49842575 | A | T | 1 | a0002c0003t0004g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.358-1709T>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49842575 | |||||||
| chr14:49842720 | T | C | 1 | a0001c0001t0002g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.358-1854A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49842720 | |||||||
| chr14:49842799 | G | A | 1 | a0001c0009t0001g0092 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.358-1933C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49842799 | |||||||
| chr14:49843048 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0002g0089 |
2 | NA18994.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.358-2182C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49843048 | |||||||
| chr14:49843385 | A | G | 1 | a0002c0002t0005g0004 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.358-2519T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49843385 | |||||||
| chr14:49843597 | G | A | 1 | a0001c0001t0002g0112 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.357+2543C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49843597 | |||||||
| chr14:49843683 | T | C | 27 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0003g0001 others(24): Show |
28 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.357+2457A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49843683 | |||||||
| chr14:49843744 | G | A | 6 | a0001c0001t0001g0052 a0001c0001t0001g0090 a0001c0001t0001g0091 others(3): Show |
6 | HG02056.hp1 HG02056.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.357+2396C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49843744 | |||||||
| chr14:49843768 | A | C | 1 | a0001c0001t0001g0158 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.357+2372T>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49843768 | |||||||
| chr14:49843828 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.357+2312C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49843828 | |||||||
| chr14:49843872 | G | A | 1 | a0001c0004t0002g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.357+2268C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49843872 | |||||||
| chr14:49844021 | C | A | 1 | a0001c0001t0001g0044 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.357+2119G>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844021 | |||||||
| chr14:49844111 | C | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0111 |
2 | NA18981.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.357+2029G>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844111 | |||||||
| chr14:49844122 | C | CA | 25 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0045 others(22): Show |
25 | HG01346.hp2 HG01433.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.357+2017dupT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844122 | |||||||
| chr14:49844134 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.357+2006G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844134 | |||||||
| chr14:49844135 | G | A | 10 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0200 others(7): Show |
10 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.357+2005C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844135 | |||||||
| chr14:49844278 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.357+1862A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844278 | |||||||
| chr14:49844307 | G | A | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+1833C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844307 | |||||||
| chr14:49844318 | C | T | 3 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 |
3 | HG00609.hp2 NA18962.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.357+1822G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844318 | |||||||
| chr14:49844407 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.357+1733C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844407 | |||||||
| chr14:49844487 | C | G | 1 | a0001c0001t0001g0052 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.357+1653G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844487 | |||||||
| chr14:49844572 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.357+1568C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844572 | |||||||
| chr14:49844613 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.357+1527G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844613 | |||||||
| chr14:49844693 | G | A | 8 | a0001c0001t0001g0155 a0001c0001t0002g0150 a0001c0001t0002g0151 others(5): Show |
8 | HG00323.hp1 HG01255.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.357+1447C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844693 | |||||||
| chr14:49844693 | GTATT | G | 13 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(10): Show |
13 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.357+1443_357+1446d others(6): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844693 | |||||||
| chr14:49844714 | TACAC | T | 54 | a0001c0001t0001g0017 a0001c0001t0001g0040 a0001c0001t0001g0050 others(51): Show |
54 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.357+1422_357+1425d others(6): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844714 | |||||||
| chr14:49844715 | ACACACGC others(3): Show |
A | 41 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0002g0019 others(38): Show |
42 | HG00280.hp1 HG00558.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.357+1415_357+1424d others(12): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844715 | |||||||
| chr14:49844717 | A | G | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(107): Show |
110 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.357+1423T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844717 | |||||||
| chr14:49844718 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG01255.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.357+1422G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844718 | |||||||
| chr14:49844721 | GCACGCGC others(1): Show |
G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0046 a0001c0001t0001g0047 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.357+1411_357+1418d others(10): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844721 | |||||||
| chr14:49844723 | A | G | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(100): Show |
103 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.357+1417T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844723 | |||||||
| chr14:49844727 | G | GCA | 5 | a0001c0001t0001g0033 a0001c0001t0002g0030 a0001c0001t0002g0031 others(2): Show |
5 | HG02280.hp1 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.357+1411_357+1412d others(4): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844727 | |||||||
| chr14:49844727 | G | GCACA | 2 | a0001c0004t0002g0036 a0001c0004t0002g0037 |
2 | HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.357+1412_357+1413i others(6): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844727 | |||||||
| chr14:49844729 | A | G | 55 | a0001c0001t0001g0017 a0001c0001t0001g0040 a0001c0001t0001g0100 others(52): Show |
55 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.357+1411T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844729 | |||||||
| chr14:49844729 | ACG | A | 8 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0108 others(5): Show |
8 | HG00544.hp1 HG01255.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.357+1409_357+1410d others(4): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844729 | |||||||
| chr14:49844729 | ACGCGCG | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(83): Show |
86 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.357+1405_357+1410d others(8): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844729 | |||||||
| chr14:49844731 | G | A | 9 | a0001c0001t0001g0033 a0001c0001t0002g0030 a0001c0001t0002g0031 others(6): Show |
9 | HG02280.hp1 HG02559.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.357+1409C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844731 | |||||||
| chr14:49844733 | G | A | 67 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0040 others(64): Show |
67 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.357+1407C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844733 | |||||||
| chr14:49844733 | G | GCACACA | 9 | a0002c0003t0004g0211 a0002c0003t0004g0212 a0002c0003t0004g0215 others(6): Show |
9 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.357+1406_357+1407i others(8): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844733 | |||||||
| chr14:49844733 | G | GCACACAC others(5): Show |
1 | a0002c0003t0004g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.357+1406_357+1407i others(14): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844733 | |||||||
| chr14:49844735 | G | A | 81 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0040 others(78): Show |
81 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.357+1405C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844735 | |||||||
| chr14:49844735 | GCGCACAC others(1): Show |
G | 3 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0007 |
3 | NA19011.hp2 NA19076.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.357+1397_357+1404d others(10): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844735 | |||||||
| chr14:49844737 | G | A | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(168): Show |
171 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.357+1403C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844737 | |||||||
| chr14:49844737 | G | GCGCACAC others(5): Show |
1 | a0002c0003t0004g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.357+1402_357+1403i others(14): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844737 | |||||||
| chr14:49844737 | GCA | G | 9 | a0001c0001t0001g0044 a0002c0002t0001g0137 a0002c0002t0001g0200 others(6): Show |
9 | HG00558.hp2 HG02145.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.357+1401_357+1402d others(4): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844737 | |||||||
| chr14:49844737 | GCACACAC others(3): Show |
G | 24 | a0001c0001t0003g0001 a0001c0001t0003g0177 a0001c0001t0003g0178 others(21): Show |
25 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.357+1393_357+1402d others(12): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844737 | |||||||
| chr14:49844737 | GCACACAC others(5): Show |
G | 1 | a0001c0001t0003g0176 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.357+1391_357+1402d others(14): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844737 | |||||||
| chr14:49844739 | A | G | 4 | a0001c0001t0001g0015 a0001c0001t0002g0014 a0001c0004t0002g0016 others(1): Show |
4 | HG00597.hp2 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.357+1401T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844739 | |||||||
| chr14:49844741 | A | G | 1 | a0002c0002t0005g0006 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.357+1399T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844741 | |||||||
| chr14:49844766 | T | C | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
4 | HG02055.hp1 HG02622.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.357+1374A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844766 | |||||||
| chr14:49844773 | T | A | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(204): Show |
208 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.357+1367A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844773 | |||||||
| chr14:49844812 | G | C | 1 | a0001c0001t0003g0193 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.357+1328C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844812 | |||||||
| chr14:49844915 | C | T | 11 | a0002c0003t0004g0210 a0002c0003t0004g0211 a0002c0003t0004g0212 others(8): Show |
11 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.357+1225G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844915 | |||||||
| chr14:49844921 | A | G | 10 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0200 others(7): Show |
10 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.357+1219T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49844921 | |||||||
| chr14:49845034 | G | T | 10 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0200 others(7): Show |
10 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.357+1106C>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49845034 | |||||||
| chr14:49845075 | A | AAGTTAGT others(1): Show |
9 | a0002c0003t0004g0210 a0002c0003t0004g0211 a0002c0003t0004g0212 others(6): Show |
9 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.357+1057_357+1064d others(10): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49845075 | |||||||
| chr14:49845075 | A | AAGTTAGT others(5): Show |
2 | a0002c0003t0004g0209 a0002c0003t0004g0217 |
2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.357+1053_357+1064d others(14): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49845075 | |||||||
| chr14:49845208 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0002g0117 |
2 | HG01361.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.357+932A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49845208 | |||||||
| chr14:49845210 | A | T | 9 | a0001c0001t0001g0041 a0001c0001t0001g0119 a0001c0001t0001g0120 others(6): Show |
9 | HG00741.hp1 HG01081.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.357+930T>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49845210 | |||||||
| chr14:49845590 | A | G | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+550T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49845590 | |||||||
| chr14:49845687 | C | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(189): Show |
193 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.357+453G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49845687 | |||||||
| chr14:49845966 | T | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.357+174A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 4/32 | chr14 | 49845966 | |||||||
| chr14:49846274 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.232-9T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49846274 | |||||||
| chr14:49846490 | G | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0017 others(26): Show |
29 | HG00280.hp2 HG00544.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.232-225C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49846490 | |||||||
| chr14:49846693 | G | C | 10 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0200 others(7): Show |
10 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.232-428C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49846693 | |||||||
| chr14:49846696 | C | A | 1 | a0001c0001t0002g0139 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.232-431G>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49846696 | |||||||
| chr14:49846745 | G | A | 1 | a0001c0001t0003g0194 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.232-480C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49846745 | |||||||
| chr14:49847047 | G | A | 1 | a0002c0002t0001g0207 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.232-782C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49847047 | |||||||
| chr14:49847120 | G | A | 1 | a0001c0005t0001g0140 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.232-855C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49847120 | |||||||
| chr14:49847706 | CTTTTTTT others(2): Show |
C | 11 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(8): Show |
11 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.232-1450_232-1442d others(11): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49847706 | |||||||
| chr14:49847706 | CTTTTTTT others(3): Show |
C | 1 | a0002c0003t0004g0216 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.232-1451_232-1442d others(12): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49847706 | |||||||
| chr14:49847706 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0018 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.232-1455_232-1442d others(16): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49847706 | |||||||
| chr14:49847706 | CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0001g0141 a0003c0008t0001g0142 |
2 | HG02040.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.232-1457_232-1442d others(18): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49847706 | |||||||
| chr14:49847893 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.232-1628C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49847893 | |||||||
| chr14:49847956 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.232-1691G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49847956 | |||||||
| chr14:49848031 | C | CA | 5 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
5 | HG00741.hp1 HG01123.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-1767dupT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49848031 | |||||||
| chr14:49848051 | A | G | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 |
3 | HG01952.hp2 HG01993.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.232-1786T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49848051 | |||||||
| chr14:49848077 | A | C | 12 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(9): Show |
12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.232-1812T>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49848077 | |||||||
| chr14:49848337 | T | C | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG00280.hp2 HG00642.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.232-2072A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49848337 | |||||||
| chr14:49848385 | T | C | 2 | a0001c0001t0003g0181 a0001c0001t0003g0182 |
2 | HG00738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.232-2120A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49848385 | |||||||
| chr14:49848661 | C | T | 37 | a0001c0001t0001g0033 a0001c0001t0001g0155 a0001c0001t0001g0164 others(34): Show |
37 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.232-2396G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49848661 | |||||||
| chr14:49848833 | C | CA | 39 | a0001c0001t0001g0155 a0001c0001t0001g0158 a0001c0001t0001g0159 others(36): Show |
40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.232-2569dupT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49848833 | |||||||
| chr14:49848860 | A | C | 1 | a0001c0001t0001g0018 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.232-2595T>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49848860 | |||||||
| chr14:49848884 | G | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02109.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.232-2619C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49848884 | |||||||
| chr14:49849033 | C | T | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(204): Show |
208 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.231+2530G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49849033 | |||||||
| chr14:49849239 | C | G | 1 | a0001c0001t0001g0017 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.231+2324G>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49849239 | |||||||
| chr14:49849355 | G | A | 1 | a0001c0001t0003g0195 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.231+2208C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49849355 | |||||||
| chr14:49849566 | T | C | 4 | a0001c0001t0003g0197 a0001c0001t0003g0198 a0001c0001t0003g0199 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+1997A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49849566 | |||||||
| chr14:49849568 | C | T | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+1995G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49849568 | |||||||
| chr14:49849939 | G | C | 25 | a0001c0001t0003g0001 a0001c0001t0003g0176 a0001c0001t0003g0177 others(22): Show |
26 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.231+1624C>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49849939 | |||||||
| chr14:49850041 | G | A | 10 | a0001c0001t0001g0164 a0001c0001t0002g0010 a0001c0001t0002g0011 others(7): Show |
10 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.231+1522C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49850041 | |||||||
| chr14:49850081 | T | C | 25 | a0001c0001t0003g0001 a0001c0001t0003g0176 a0001c0001t0003g0177 others(22): Show |
26 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.231+1482A>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49850081 | |||||||
| chr14:49850342 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0002g0014 a0001c0004t0002g0016 |
3 | HG02615.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.231+1221G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49850342 | |||||||
| chr14:49850358 | A | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(204): Show |
208 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.231+1205T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49850358 | |||||||
| chr14:49850379 | C | T | 1 | a0001c0001t0009g0013 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.231+1184G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49850379 | |||||||
| chr14:49850692 | A | G | 3 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 |
3 | HG00609.hp2 NA18962.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.231+871T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49850692 | |||||||
| chr14:49850862 | C | T | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(204): Show |
208 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.231+701G>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49850862 | |||||||
| chr14:49851043 | A | G | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+520T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49851043 | |||||||
| chr14:49851280 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.231+283C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49851280 | |||||||
| chr14:49851373 | A | G | 12 | a0002c0003t0004g0209 a0002c0003t0004g0210 a0002c0003t0004g0211 others(9): Show |
12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.231+190T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 3/32 | chr14 | 49851373 | |||||||
| chr14:49851740 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.128+67C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 2/32 | chr14 | 49851740 | |||||||
| chr14:49851945 | T | A | 7 | a0002c0003t0004g0215 a0002c0003t0004g0216 a0002c0003t0004g0217 others(4): Show |
7 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.60-70A>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 1/32 | chr14 | 49851945 | |||||||
| chr14:49852025 | T | G | 1 | a0001c0001t0001g0172 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.60-150A>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 1/32 | chr14 | 49852025 | |||||||
| chr14:49852160 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.60-285A>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 1/32 | chr14 | 49852160 | |||||||
| chr14:49852171 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.60-296C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 1/32 | chr14 | 49852171 | |||||||
| chr14:49852173 | GA | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(204): Show |
208 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.60-299delT | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 1/32 | chr14 | 49852173 | |||||||
| chr14:49852213 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.60-338T>C | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 1/32 | chr14 | 49852213 | |||||||
| chr14:49852289 | G | T | 169 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(166): Show |
169 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.59+406C>A | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 1/32 | chr14 | 49852289 | |||||||
| chr14:49852294 | G | GCTCT | 4 | a0002c0002t0005g0004 a0002c0002t0005g0005 a0002c0002t0005g0006 others(1): Show |
4 | HG00597.hp2 NA19011.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+397_59+400dupAG others(2): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 1/32 | chr14 | 49852294 | |||||||
| chr14:49852491 | A | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
2 | HG02135.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.59+204T>G | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 1/32 | chr14 | 49852491 | |||||||
| chr14:49852594 | G | A | 8 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.59+101C>T | NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 1/32 | chr14 | 49852594 |